US20050008712A1 - Compositions incorporating high-caffeine green tea extract and related methods for promoting healthy body weight - Google Patents
Compositions incorporating high-caffeine green tea extract and related methods for promoting healthy body weight Download PDFInfo
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- US20050008712A1 US20050008712A1 US10/615,887 US61588703A US2005008712A1 US 20050008712 A1 US20050008712 A1 US 20050008712A1 US 61588703 A US61588703 A US 61588703A US 2005008712 A1 US2005008712 A1 US 2005008712A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/82—Theaceae (Tea family), e.g. camellia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
- A61K31/353—3,4-Dihydrobenzopyrans, e.g. chroman, catechin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
- A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7048—Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
Definitions
- the present invention generally relates to providing a method or compound for promoting healthy body weight, increasing energy level and improving a variety of related physiological factors and, more particularly, to providing a composition that includes effective amounts of EGCG and caffeine derived from green tea to further promote healthy body weight, increase energy level and improve a variety of related physiological factors and a method of administering the composition.
- Increase in body weight results from an imbalance between energy intake and expenditure in a person, manifested by excessive expansion of adipose tissue mass in the person.
- Obesity leads to a number of poor health factors. In particular, obesity increases the risk of high blood pressure, hypertension, type II diabetes, arthritis, elevated cholesterol, and cancer. Although 30-40% of obese people claim they are trying to lose or maintain body weight, their success rate is low. Dietary approaches for the management of excess body weight have been unsuccessful due to improper caloric restriction and/or lack of physical exercise. Low calorie diets can provide for temporary weight loss, but they have not proven themselves as long-term solutions for people trying to lose or maintain weight. Drugs that suppress appetite, reduce food intake, increase energy expenditure and/or affect nutrient partitioning or metabolism have potential efficacy in reducing body weight. Unfortunately, these also frequently are accompanied by adverse side effects, some of which are life threatening.
- High blood cholesterol, high blood triglyceride levels, and obesity all are indicators of increased risk for heart disease and other health maladies.
- high levels of total cholesterol, LDL cholesterol or triglycerides, as well as low levels of HDL cholesterol all are risk factors for various cardiovascular diseases. These conditions are exacerbated by many factors, including poor diet, lack of exercise and obesity. Prevalence for obesity can be reflected in excessive eating and also by genetic factors.
- One method for reducing appetite, and therefore excessive eating is by raising serotonin levels in a person.
- Increased brain levels of serotonin an important neurotransmitter involved in proper brain function, including regulation of sleep and mood, have also been linked with appetite suppression.
- a known biomarker for genetic propensity of a person toward obesity is serum leptin, a hormone encoded by the gene that regulates body weight. Leptin binds to receptors in the brain, where it activates signals that inhibit food intake and increase energy expenditure. Studies have shown that plasma leptin levels are higher in overweight than in non-overweight individuals, and higher in women than in men.
- the methods described above to treat obesity in humans may be applicable to treating other mammals as well, including animals commonly kept as pets, such as dogs and cats.
- Excess body weight has reached epidemic proportions in, and is the most common nutritional disorder among, pets. It is estimated that 50% of pets (or roughly 60 million animals) in the United States are overweight or obese (a weight ten percent over ideal body weight is considered overweight, and a weight twenty percent over ideal body weight is clinically defined as obese).
- An extra five pounds on a dog that should weigh 17 pounds or an extra three pounds on a cat that should weight 10 pounds is comparable to an extra 50 pounds on a person who should weigh 170 pounds.
- Overweight pets are at higher risk of developing health problems such as heart disease, skeletal problems, breathing problems, diabetes and arthritis.
- weight management in veterinary medicine relies on one or more recommendations.
- a veterinarian may prescribe high fiber/reduced calorie diets, or advocate other dietary changes focusing on a decrease in overall caloric intake.
- Another method to manage pet weight is to increase exercise. Untreated obesity can be a devastating condition for a pet, and instituting an obesity-management program will add quality years to a pet's life.
- leptin level is a 167 amino acid protein hormone encoded by the gene that regulates body weight. Synthesized and secreted by adipocytes (fat cells), leptin binds to receptors in the brain, where it activates signals that inhibit food intake and increase energy expenditure. When receptor-binding activity is diminished, a condition called “leptin resistance,” plasma leptin levels increase and the leptin loses its ability to inhibit food intake and increase energy expenditure. Studies have shown that plasma leptin levels are higher in overweight than in non-overweight individuals, and higher in women than in men.
- Leptin is synthesized and secreted by adipocytes, is present in the bloodstream in amounts related to the amount of fat in the body, and acts primarily on the brain to regulate food intake. Leptin has been shown to be able to modulate insulin secretion and action through these receptors.
- Fat metabolites are products of fat degradation. Following exercise or other fat “burning” processes, fat tissue breaks down into small molecular components, including malondialdehyde, formaldehyde, acetaldehyde and acetone. Increased urinary levels of fat metabolites indicates increased fat degradation or “burning,” which can result in weight loss.
- serum serotonin level affects eating behavior and body weight. Increased plasma levels of serotonin are associated with decreased food intake, reduced weight gain and increased energy expenditure. Because serotonin has been implicated in the regulation of eating behavior and body weight regulation, appetite suppression could be mediated by this serotonin.
- caffeine One chemical known to promote weight loss is caffeine.
- Caffeine or trimethylxanthine (C 8 H 10 N 4 O 2 ), acts as a mild stimulant to the central nervous system when ingested by persons in amounts up to about 300 mg. Higher levels of caffeine consumption can lead to headache, nervousness and loss of sleep. Caffeine also exhibits effects that indicate it may serve as a mild appetite suppressant. Additionally, caffeine is believed to increase metabolism and bum calories by a process known as “thermogenesis,” and it also acts as a diuretic to remove excess fluids from a person. Common sources of caffeine include coffee and tea. Despite its weight loss properties, caffeine often is removed from these products prior to consumption, as people seek to reduce caffeine consumption for health reasons.
- tea Besides caffeine, tea, and particularly green tea, includes polyphenols having a variety of known beneficial effects.
- the main polyphenol of green tea is ( ⁇ )-epigallo-catechin-3-gallate (EGCG).
- EGCG is a potent antioxidant and anti-neoplastic agent.
- Green tea catechins such as EGCG have been shown to inhibit lipid oxidation in low-density lipoprotein and provide a variety of antioxidant effects.
- Green tea incorporating EGCG also is known to possess thermogenic properties, increasing energy expenditure and fat oxidation in humans. In particular, it plays a role in the control of body composition via sympathetic activation of thermogenic fat oxidation.
- EGCG significantly reduces food intake, body weight, blood cholesterol and triglycerides in rats.
- the rats were injected with pure green tea catechin to study its effects on the endocrine systems of the rats.
- EGCG was found to significantly reduced food intake and body weight in the rats. Similar effects were observed in both lean and obese male Zucker rats, suggesting that the effect of EGCG was independent of an intact leptin receptor.
- EGCG may interact specifically with a component of a leptin (i.e., the so-called “obesity gene”) independent of its appetite control pathway.
- these researchers also have shown that EGCG injected into rats caused the animals to lose 20% of their body weight after daily injections for a week.
- the present invention resides in an improved method and composition for promoting healthy body weight, increasing energy level and improving a variety of related physiological factors.
- the method and composition of the present invention utilizes amounts of EGCG and caffeine that work synergistically to further promote healthy body weight, increase energy level and improve various physiological factors.
- the method of the present invention includes administering to those persons or other mammals effective amounts of a composition incorporating EGCG and caffeine derived from green tea.
- the composition of the present invention comprises EGCG and caffeine in a ratio by weight between 1.0:0.20 and 1.0:9.0, respectively, or between about 10% and about 80% by weight of EGCG and about 20% and 90% by weight of caffeine.
- the composition is in the form of a pill, tablet, capsule, lozenge, gum, food, oral spray, beverage, toothpaste, powder or other orally administered form or in the form of an absorbent patch.
- the method of the present invention comprises administering to the person or other mammal a composition comprising EGCG and caffeine derived from the Camellia sinensis plant in a ratio by weight between 1.0:0.20 and 1.0:9.0, respectively, in an amount sufficient to reduce excess, or maintain healthy, body weight in the person or other mammal.
- the method of the invention includes causing a person or other mammal to come into contact with EGCG and caffeine, where the ratio by weight of the EGCG to the caffeine is between 1.0:0.20 and 1.0:4.0, respectively.
- the present invention includes an amount of EGCG and caffeine that separately or together come into contact with a person or another mammal, where the ratio by weight of the EGCG to the caffeine is between 1.0:0.20 and 1.0:9.0, respectively.
- the EGCG and caffeine of the method and composition are derived from the Camellia sinensis plant.
- the step of administering comprises administering approximately 270 milligrams of EGCG and 270 milligrams of caffeine daily.
- the step of administering comprises administering the composition daily in three substantially equally divided does, approximately 30 to 60 minutes before meals.
- the method of present invention further includes administering to the person or other mammal a composition comprising EGCG and caffeine in a ratio by weight between 1.0:0.20 and 1.0:4.0, respectively, in an amount sufficient to provide energy in an expiatory manner to the person or other mammal.
- the method of the present invention further includes identifying at least one person or other mammal that can benefit from an increase in energy.
- the present invention resides in compositions incorporating green tea extract incorporating EGCG, as well as caffeine, in ratios not previously shown. Specifically, EGCG and caffeine are present in the compositions in a preferred ratio of about 1:1.
- the caffeine in these tea extract compositions is provided is endogenous; i.e., it is caffeine naturally derived from the green tea used to make the extract, instead of being provided from an outside source, whether natural or synthetic.
- the present invention also resides in methods for controlling body weight, providing immediate expiatory energy, and improving the above-discussed health factors of persons or other mammals, including increasing serum serotonin levels, reducing serum leptin levels, increasing fat oxidation, reducing food intake, and lowering body mass index (BMI).
- the methods include identifying a person or other mammal who is, or is at risk for being, overweight, or who would benefit either from increased energy levels or the above-described physiological changes, and administering to the person or other mammal a composition comprising sufficient amounts of green tea extract incorporating EGCG along with caffeine, in an amount sufficient to be effective.
- compositions of the present invention incorporate endogenous caffeine, which provides several commercial advantages, including: 1) endogenous green tea caffeine is natural, which is preferred to synthetic sources, 2) it is less expensive and results in a smaller capsule or less capsule fill than adding exogenous natural sources, such as from guarana or gotu-kola, and 3) it provides certain product labeling advantages, including not having to list exogenous sources of caffeine on the ingredients panel.
- EGCG and caffeine are present in the composition in a ratio of between 1.0:0.20 and 1.0:9.0 more preferably 1.0:0.25 and 1.0:4.0, and most preferably about 1.0:1.0.
- EGCG and caffeine preferably are derived from an extract of green tea ( Camellia sinensis ), though other sources of EGCG and caffeine can be used.
- the composition preferably incorporates at least 10% to 80% EGCG and 20% to 90% caffeine, more preferably 30% to 50% each of EGCG and caffeine, and most preferably about 30% each of EGCG and caffeine.
- compositions of the present invention provide for the safe, effective and convenient reduction of excess body weight and resulting reduction in body mass index (BMI), or maintenance of healthy body weight and healthy BMI, in persons or other mammals. Besides these effects, administration of the compositions also provides for reducing serum leptin levels, increasing serum serotonin levels, reducing food intake, increasing fat oxidation, decreasing elevated total and LDL cholesterol, increasing HDL cholesterol, and reducing elevated triglyceride levels in persons or other mammals that would benefit from such effects.
- BMI body mass index
- compositions incorporating EGCG along with a similar or identical amount of caffeine when administered to persons in sufficient quantities, provide for superior improvement in reducing excess body weight and improving the related health factors described above than was expected, based on the previously know properties of the two components. These compositions also provide for superior energy increase in persons consuming them.
- the combination of EGCG and caffeine in these ratios can reduce body weight, lower body mass index, increase serum serotonin levels, reduce food intake, reduce serum leptin levels, increase fat oxidation, decrease harmful total and LDL cholesterol, increase beneficial HDL cholesterol and lower triglycerides significantly greater than either EGCG alone, or EGCG and caffeine in previously-administered amounts.
- the composition also provides an expiatory (i.e., immediate) increase in perceived energy level in a person consuming it.
- the preferred composition includes 540 mg of EGCG and caffeine, preferably in a 1.0:1.0 ratio by weight (i.e., 270 mg of EGCG and 270 mg of caffeine).
- the composition also can include inert ingredients or diluents, such as sugar, maltodextrin, cellulose, or other inert ingredients commonly used in dietary supplements and food and beverage products.
- the composition may be in various forms, including those commonly used for dietary supplements (e.g., pill, tablet, capsule, lozenge, gum, food, absorbent patch, oral spray, beverage, toothpaste, or powder).
- composition also can be incorporated into food or beverage products, including bars, shakes, gums, beverages, or other processed or prepared food or beverage products, or any other orally administerable form.
- the composition preferably is administered daily in three substantially equally divided doses, approximately 30 to 60 minutes before meals.
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Abstract
Methods for promoting healthy body weight, increasing energy level and improving a variety of related physiological factors include administering to those persons or other mammals effective amounts of a composition incorporating EGCG and caffeine derived from green tea, preferably in equal or nearly equal amounts. The EGCG and caffeine in these amounts work synergistically to further promote healthy body weight, increase energy level and improve these physiological factors.
Description
- The present invention generally relates to providing a method or compound for promoting healthy body weight, increasing energy level and improving a variety of related physiological factors and, more particularly, to providing a composition that includes effective amounts of EGCG and caffeine derived from green tea to further promote healthy body weight, increase energy level and improve a variety of related physiological factors and a method of administering the composition.
- Excess body weight is becoming more prevalent worldwide at an alarming rate, both in developing and developed countries. Approximately 61 percent of adults in the U.S. are overweight (i.e., having a body mass index (BMI) of greater than 25 kg/m2), while more than 26 percent of U.S. adults are obese (i.e., having a BMI of greater than 30 kg/m2). Obesity is the second leading cause of premature death in the U.S. Approximately 300,000 Americans die each year from complications caused by obesity. According to the World Health Organization, there are over 300 million obese adults worldwide. Environmental and behavioral changes brought about by economic development, modernization and urbanization have been linked to the global rise in obesity in adults and children, the true health consequences of which may not be fully known for years to come. Consumption of western-style diets, low levels of physical activity and sedentary lifestyles generally have been implicated in the worldwide trend of weight gain.
- Increase in body weight results from an imbalance between energy intake and expenditure in a person, manifested by excessive expansion of adipose tissue mass in the person. Obesity leads to a number of poor health factors. In particular, obesity increases the risk of high blood pressure, hypertension, type II diabetes, arthritis, elevated cholesterol, and cancer. Although 30-40% of obese people claim they are trying to lose or maintain body weight, their success rate is low. Dietary approaches for the management of excess body weight have been unsuccessful due to improper caloric restriction and/or lack of physical exercise. Low calorie diets can provide for temporary weight loss, but they have not proven themselves as long-term solutions for people trying to lose or maintain weight. Drugs that suppress appetite, reduce food intake, increase energy expenditure and/or affect nutrient partitioning or metabolism have potential efficacy in reducing body weight. Unfortunately, these also frequently are accompanied by adverse side effects, some of which are life threatening.
- High blood cholesterol, high blood triglyceride levels, and obesity all are indicators of increased risk for heart disease and other health maladies. In particular, high levels of total cholesterol, LDL cholesterol or triglycerides, as well as low levels of HDL cholesterol, all are risk factors for various cardiovascular diseases. These conditions are exacerbated by many factors, including poor diet, lack of exercise and obesity. Prevalence for obesity can be reflected in excessive eating and also by genetic factors. One method for reducing appetite, and therefore excessive eating, is by raising serotonin levels in a person. Increased brain levels of serotonin, an important neurotransmitter involved in proper brain function, including regulation of sleep and mood, have also been linked with appetite suppression. Also, a known biomarker for genetic propensity of a person toward obesity is serum leptin, a hormone encoded by the gene that regulates body weight. Leptin binds to receptors in the brain, where it activates signals that inhibit food intake and increase energy expenditure. Studies have shown that plasma leptin levels are higher in overweight than in non-overweight individuals, and higher in women than in men.
- The methods described above to treat obesity in humans may be applicable to treating other mammals as well, including animals commonly kept as pets, such as dogs and cats. Excess body weight has reached epidemic proportions in, and is the most common nutritional disorder among, pets. It is estimated that 50% of pets (or roughly 60 million animals) in the United States are overweight or obese (a weight ten percent over ideal body weight is considered overweight, and a weight twenty percent over ideal body weight is clinically defined as obese). An extra five pounds on a dog that should weigh 17 pounds or an extra three pounds on a cat that should weight 10 pounds is comparable to an extra 50 pounds on a person who should weigh 170 pounds. Overweight pets are at higher risk of developing health problems such as heart disease, skeletal problems, breathing problems, diabetes and arthritis. Traditionally, weight management in veterinary medicine relies on one or more recommendations. A veterinarian may prescribe high fiber/reduced calorie diets, or advocate other dietary changes focusing on a decrease in overall caloric intake. Another method to manage pet weight is to increase exercise. Untreated obesity can be a devastating condition for a pet, and instituting an obesity-management program will add quality years to a pet's life.
- Various methods exist for treating obesity and the other related health factors discussed above, such as improved diet, increased exercise, and various medications. These, however, have not been entirely effective treatments. Diet modification and increased exercise can be difficult for some individuals to maintain for an extended period, and medications introduce the possibility of negative side effects.
- A variety of biological factors are relevant to regulation of body weight in persons. One of these is leptin level. Leptin is a 167 amino acid protein hormone encoded by the gene that regulates body weight. Synthesized and secreted by adipocytes (fat cells), leptin binds to receptors in the brain, where it activates signals that inhibit food intake and increase energy expenditure. When receptor-binding activity is diminished, a condition called “leptin resistance,” plasma leptin levels increase and the leptin loses its ability to inhibit food intake and increase energy expenditure. Studies have shown that plasma leptin levels are higher in overweight than in non-overweight individuals, and higher in women than in men. Leptin is synthesized and secreted by adipocytes, is present in the bloodstream in amounts related to the amount of fat in the body, and acts primarily on the brain to regulate food intake. Leptin has been shown to be able to modulate insulin secretion and action through these receptors. These findings confirm earlier observations of higher leptin levels in obese individuals than in lean individuals.
- Another important factor in regulating body weight is fat metabolysis. Fat metabolites are products of fat degradation. Following exercise or other fat “burning” processes, fat tissue breaks down into small molecular components, including malondialdehyde, formaldehyde, acetaldehyde and acetone. Increased urinary levels of fat metabolites indicates increased fat degradation or “burning,” which can result in weight loss.
- Also, serum serotonin level affects eating behavior and body weight. Increased plasma levels of serotonin are associated with decreased food intake, reduced weight gain and increased energy expenditure. Because serotonin has been implicated in the regulation of eating behavior and body weight regulation, appetite suppression could be mediated by this serotonin.
- One chemical known to promote weight loss is caffeine. Caffeine, or trimethylxanthine (C8H10N4O2), acts as a mild stimulant to the central nervous system when ingested by persons in amounts up to about 300 mg. Higher levels of caffeine consumption can lead to headache, nervousness and loss of sleep. Caffeine also exhibits effects that indicate it may serve as a mild appetite suppressant. Additionally, caffeine is believed to increase metabolism and bum calories by a process known as “thermogenesis,” and it also acts as a diuretic to remove excess fluids from a person. Common sources of caffeine include coffee and tea. Despite its weight loss properties, caffeine often is removed from these products prior to consumption, as people seek to reduce caffeine consumption for health reasons.
- Besides caffeine, tea, and particularly green tea, includes polyphenols having a variety of known beneficial effects. In particular, the main polyphenol of green tea is (−)-epigallo-catechin-3-gallate (EGCG). EGCG is a potent antioxidant and anti-neoplastic agent. Green tea catechins such as EGCG have been shown to inhibit lipid oxidation in low-density lipoprotein and provide a variety of antioxidant effects. Green tea incorporating EGCG also is known to possess thermogenic properties, increasing energy expenditure and fat oxidation in humans. In particular, it plays a role in the control of body composition via sympathetic activation of thermogenic fat oxidation. A previous study showed that relative placebo treatment with green tea extract resulted in a 4% increase in 24-hour Energy Expenditure and a significant decrease in 24-hour Respiratory Quotient from 0.88 to 0.85, without any change in urinary nitrogen. Twenty-four hour urinary norepinephrine excretion was higher during treatment with the green tea extract than with the placebo by an average of 40%. For comparison, treatment with caffeine in amounts equivalent to those naturally occurring in the green tea extract had no significant effect on any of these measured factors.
- Another study demonstrated that EGCG significantly reduces food intake, body weight, blood cholesterol and triglycerides in rats. For clear assessment of the possible physiological effects of green tea consumption, the rats were injected with pure green tea catechin to study its effects on the endocrine systems of the rats. EGCG was found to significantly reduced food intake and body weight in the rats. Similar effects were observed in both lean and obese male Zucker rats, suggesting that the effect of EGCG was independent of an intact leptin receptor. EGCG may interact specifically with a component of a leptin (i.e., the so-called “obesity gene”) independent of its appetite control pathway. These researchers also have shown that EGCG injected into rats caused the animals to lose 20% of their body weight after daily injections for a week.
- Both caffeine and EGCG are known to exhibit some weight control properties in persons or other mammals consuming them. However, conventional administration of these does not provide weight loss that is fully satisfactory. It is apparent from the above that a need exists for improved methods and compositions for controlling body weight and improving the health condition of persons or other mammals prone to excess body weight, including improvement of body mass index (an indicator of healthy body weight), serum leptin levels, and the cardiovascular risk factors total cholesterol, LDL cholesterol, HDL cholesterol and triglycerides. The present invention fulfills this need and provides further related advantages.
- The present invention resides in an improved method and composition for promoting healthy body weight, increasing energy level and improving a variety of related physiological factors. The method and composition of the present invention utilizes amounts of EGCG and caffeine that work synergistically to further promote healthy body weight, increase energy level and improve various physiological factors.
- In a more detailed feature of the invention, the method of the present invention includes administering to those persons or other mammals effective amounts of a composition incorporating EGCG and caffeine derived from green tea.
- In yet another more detailed feature of the invention, the composition of the present invention comprises EGCG and caffeine in a ratio by weight between 1.0:0.20 and 1.0:9.0, respectively, or between about 10% and about 80% by weight of EGCG and about 20% and 90% by weight of caffeine.
- In yet another more detailed feature of the invention, the composition is in the form of a pill, tablet, capsule, lozenge, gum, food, oral spray, beverage, toothpaste, powder or other orally administered form or in the form of an absorbent patch.
- In yet another more detailed feature of the invention, the method of the present invention comprises administering to the person or other mammal a composition comprising EGCG and caffeine derived from the Camellia sinensis plant in a ratio by weight between 1.0:0.20 and 1.0:9.0, respectively, in an amount sufficient to reduce excess, or maintain healthy, body weight in the person or other mammal.
- In yet another more detailed feature of the invention, the method of the invention includes causing a person or other mammal to come into contact with EGCG and caffeine, where the ratio by weight of the EGCG to the caffeine is between 1.0:0.20 and 1.0:4.0, respectively.
- In yet another more detailed feature of the invention, the present invention includes an amount of EGCG and caffeine that separately or together come into contact with a person or another mammal, where the ratio by weight of the EGCG to the caffeine is between 1.0:0.20 and 1.0:9.0, respectively.
- In yet another more detailed feature of the invention, the EGCG and caffeine of the method and composition are derived from the Camellia sinensis plant.
- In yet another more detailed feature of the invention, the step of administering comprises administering approximately 270 milligrams of EGCG and 270 milligrams of caffeine daily.
- In yet another more detailed feature of the invention, the step of administering comprises administering the composition daily in three substantially equally divided does, approximately 30 to 60 minutes before meals.
- In yet another more detailed feature of the invention, the method of present invention further includes administering to the person or other mammal a composition comprising EGCG and caffeine in a ratio by weight between 1.0:0.20 and 1.0:4.0, respectively, in an amount sufficient to provide energy in an expiatory manner to the person or other mammal.
- In yet another more detailed feature of the invention, the method of the present invention further includes identifying at least one person or other mammal that can benefit from an increase in energy.
- The present invention resides in compositions incorporating green tea extract incorporating EGCG, as well as caffeine, in ratios not previously shown. Specifically, EGCG and caffeine are present in the compositions in a preferred ratio of about 1:1. The caffeine in these tea extract compositions is provided is endogenous; i.e., it is caffeine naturally derived from the green tea used to make the extract, instead of being provided from an outside source, whether natural or synthetic. The present invention also resides in methods for controlling body weight, providing immediate expiatory energy, and improving the above-discussed health factors of persons or other mammals, including increasing serum serotonin levels, reducing serum leptin levels, increasing fat oxidation, reducing food intake, and lowering body mass index (BMI). The methods include identifying a person or other mammal who is, or is at risk for being, overweight, or who would benefit either from increased energy levels or the above-described physiological changes, and administering to the person or other mammal a composition comprising sufficient amounts of green tea extract incorporating EGCG along with caffeine, in an amount sufficient to be effective.
- As discussed above, the compositions of the present invention incorporate endogenous caffeine, which provides several commercial advantages, including: 1) endogenous green tea caffeine is natural, which is preferred to synthetic sources, 2) it is less expensive and results in a smaller capsule or less capsule fill than adding exogenous natural sources, such as from guarana or gotu-kola, and 3) it provides certain product labeling advantages, including not having to list exogenous sources of caffeine on the ingredients panel. EGCG and caffeine are present in the composition in a ratio of between 1.0:0.20 and 1.0:9.0 more preferably 1.0:0.25 and 1.0:4.0, and most preferably about 1.0:1.0. These ratios are far different from the natural ratios of these components in green tea, in which caffeine levels typically are at least an order of magnitude below EGCG levels. Additionally, a number of published references and available products actually teach that the green tea extract should be decaffeinated, further reducing caffeine levels. EGCG and caffeine preferably are derived from an extract of green tea (Camellia sinensis), though other sources of EGCG and caffeine can be used. In particular, the composition preferably incorporates at least 10% to 80% EGCG and 20% to 90% caffeine, more preferably 30% to 50% each of EGCG and caffeine, and most preferably about 30% each of EGCG and caffeine.
- The methods and compositions of the present invention provide for the safe, effective and convenient reduction of excess body weight and resulting reduction in body mass index (BMI), or maintenance of healthy body weight and healthy BMI, in persons or other mammals. Besides these effects, administration of the compositions also provides for reducing serum leptin levels, increasing serum serotonin levels, reducing food intake, increasing fat oxidation, decreasing elevated total and LDL cholesterol, increasing HDL cholesterol, and reducing elevated triglyceride levels in persons or other mammals that would benefit from such effects.
- It has been surprisingly found that compositions incorporating EGCG along with a similar or identical amount of caffeine, when administered to persons in sufficient quantities, provide for superior improvement in reducing excess body weight and improving the related health factors described above than was expected, based on the previously know properties of the two components. These compositions also provide for superior energy increase in persons consuming them. Specifically, the combination of EGCG and caffeine in these ratios can reduce body weight, lower body mass index, increase serum serotonin levels, reduce food intake, reduce serum leptin levels, increase fat oxidation, decrease harmful total and LDL cholesterol, increase beneficial HDL cholesterol and lower triglycerides significantly greater than either EGCG alone, or EGCG and caffeine in previously-administered amounts. The composition also provides an expiatory (i.e., immediate) increase in perceived energy level in a person consuming it.
- Preferred administration of the composition is orally, in three equally-divided doses roughly 30 to 60 minutes before meals administered daily. For an adult, the preferred composition includes 540 mg of EGCG and caffeine, preferably in a 1.0:1.0 ratio by weight (i.e., 270 mg of EGCG and 270 mg of caffeine). The composition also can include inert ingredients or diluents, such as sugar, maltodextrin, cellulose, or other inert ingredients commonly used in dietary supplements and food and beverage products. The composition may be in various forms, including those commonly used for dietary supplements (e.g., pill, tablet, capsule, lozenge, gum, food, absorbent patch, oral spray, beverage, toothpaste, or powder). The composition also can be incorporated into food or beverage products, including bars, shakes, gums, beverages, or other processed or prepared food or beverage products, or any other orally administerable form. The composition preferably is administered daily in three substantially equally divided doses, approximately 30 to 60 minutes before meals.
- Although the invention has been disclosed in detail with reference only to the preferred embodiments, those skilled in the art will appreciate that additional methods and compositions can be made without departing from the scope of the invention.
Claims (29)
1. A composition comprising EGCG and caffeine in a ratio by weight between 1.0:0.20 and 1.0:9.0, respectively.
2. A composition as defined in claim 1 , wherein the EGCG and caffeine are derived from the Camellia sinensis plant.
3. A composition as defined in claim 1 , wherein the EGCG and caffeine are present in a ratio by weight between 1.0:0.25 and 1.0:4.0, respectively.
4. A composition as defined in claim 1 , wherein the EGCG and caffeine are present in a ratio by weight of about 1.0:1.0, respectively.
5. A composition as defined in claim 1 , wherein the ECGC and caffeine are derived from sources other than the Camellia sinensis plant.
6. A composition as defined in claim 1 , wherein the composition is in the form of a pill, tablet, capsule, lozenge, gum, food, oral spray, beverage, toothpaste, powder or other orally administered form.
7. A composition as defined in claim 1 , wherein the composition is in the form of an absorbent patch.
8. A composition as defined in claim 1 , wherein the composition comprises between about 10% and about 80% by weight of EGCG and about 20% and 90% by weight of caffeine.
9. A composition as defined in claim 8 , wherein the composition comprises 30% to 50% by weight of EGCG and 30% to 50% by weight of caffeine.
10. A composition as defined in claim 9 , wherein the composition comprises
about 30% by weight of EGCG and about 30% by weight of caffeine.
11. A method for reducing excess, or maintaining healthy, body weight in a person or other mammal comprising:
administering to the person or other mammal a composition comprising EGCG and caffeine derived from the Camellia sinensis plant in a ratio by weight between 1.0:0.20 and 1.0:9.0, respectively, in an amount sufficient to reduce excess, or maintain healthy, body weight in the person or other mammal.
12. A method as defined in claim 11 , wherein the EGCG and caffeine are present in a ratio by weight between 1.0:0.25 and 1.0:4.0, respectively.
13. A method as defined in claim 12 , wherein the EGCG and caffeine are present in a ratio by weight of about 1.0:1.0, respectively.
14. A method as defined in claim 11 , wherein the EGCG and caffeine are derived from sources other than the Camellia sinensis plant.
15. A method as defined in claim 11 , wherein the step of administering comprises administering approximately 270 milligrams of EGCG and 270 milligrams of caffeine daily.
16. A method as defined in claim 11 , wherein the step of administering comprises administering the composition daily in three substantially equally divided doses, approximately 30 to 60 minutes before meals.
17. A method as defined is claim 16 , wherein the step of administering comprises administering the composition orally.
18. A method as defined is claim 11 , further comprising identifying a person or other mammal suffering, or at risk of suffering from excess body weight.
19. A method for providing energy in an expiatory manner to a person or other mammal comprising:
administering to the person or other mammal a composition comprising EGCG and caffeine in a ratio by weight between 1.0:0.20 and 1.0:4.0, respectively, in an amount sufficient to provide energy in an expiatory manner to the person or other mammal.
20. A method as defined in claim 19 , wherein the EGCG and caffeine are present in a ratio by weight between 1.0:0.25 and 1.0:4.0, respectively.
21. A method as defined in claim 19 , wherein the EGCG and caffeine are present in a ratio by weight of about 1.0:1.0, respectively.
22. A method as defined in claim 19 , wherein the EGCG and caffeine are derived from the Camellia sinensis plant.
23. A method as defined in claim 19 , wherein the step of administering comprises administering approximately 270 milligrams of EGCG and 270 milligrams of caffeine daily.
24. A method as defined in claim 19 , wherein the step of administering comprises administering the composition daily in three substantially equally divided doses, approximately 30 to 60 minutes before meals.
25. A method as defined is claim 19 , wherein the step of administering comprises administering the composition orally.
26. A method as defined is claim 19 , further comprising identifying a person or other mammal that can benefit from an increase in energy.
27. A method for reducing excess, or maintaining healthy, body weight in a person or other mammal comprising:
causing a person or other mammal to come into contact with EGCG and caffeine, wherein the ratio by weight of the EGCG to the caffeine is between 1.0:0.20 and 1.0:4.0, respectively.
28. A method as in claim 27 , further comprising providing, either separately or together, EGCG and caffeine.
29. An amount of EGCG and caffeine that separately or together come into contact with a person or another mammal, wherein the ratio by weight of the EGCG to the caffeine is between 1.0:0.20 and 1.0:9.0, respectively.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/615,887 US20050008712A1 (en) | 2003-07-08 | 2003-07-08 | Compositions incorporating high-caffeine green tea extract and related methods for promoting healthy body weight |
AU2003258003A AU2003258003A1 (en) | 2003-07-08 | 2003-07-30 | Compositions incorporating high-caffeine green tea extract and related methods for promoting healthy body weight |
PCT/US2003/024155 WO2005014020A1 (en) | 2003-07-08 | 2003-07-30 | Compositions incorporating high-caffeine green tea extract and related methods for promoting healthy body weight |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US10/615,887 US20050008712A1 (en) | 2003-07-08 | 2003-07-08 | Compositions incorporating high-caffeine green tea extract and related methods for promoting healthy body weight |
Publications (1)
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US20050008712A1 true US20050008712A1 (en) | 2005-01-13 |
Family
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Family Applications (1)
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US10/615,887 Abandoned US20050008712A1 (en) | 2003-07-08 | 2003-07-08 | Compositions incorporating high-caffeine green tea extract and related methods for promoting healthy body weight |
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US (1) | US20050008712A1 (en) |
AU (1) | AU2003258003A1 (en) |
WO (1) | WO2005014020A1 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060173070A1 (en) * | 2005-01-31 | 2006-08-03 | Kao Corporation | Method of enhancing motor function |
US20070178216A1 (en) * | 2006-02-02 | 2007-08-02 | Chithan Kandaswami | Composition and method for promoting weight loss |
US20070178176A1 (en) * | 2006-02-02 | 2007-08-02 | Chithan Kandaswami | Composition and method for promoting weight loss |
US20070292560A1 (en) * | 2004-06-24 | 2007-12-20 | Danyi Quan | Green tea formulations and methods of preparation |
EP1885453A1 (en) * | 2005-06-03 | 2008-02-13 | Horizon Science Pty. Ltd. | Substances having body mass redistribution properties |
EP3285789A4 (en) * | 2015-04-24 | 2019-01-23 | Grethe Stoa Birketvedt | Plant extracts for the treatment of excess weight and obesity |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006131326A2 (en) * | 2005-06-07 | 2006-12-14 | Dsm Ip Assets B.V. | Novel use of (-)-epigallocatechin gallate |
PT1942874E (en) | 2005-11-04 | 2013-12-16 | Inqpharm Group Sdn Bhd | Herbal composition for weight management |
EP1961310A1 (en) * | 2007-02-01 | 2008-08-27 | DSMIP Assets B.V. | Novel use of (-) -epigallocatechin gallate |
WO2012087486A1 (en) * | 2010-12-20 | 2012-06-28 | Hill's Pet Nutrition, Inc. | Pet food compositions for inducing a satiety response |
CN112603953A (en) * | 2020-12-07 | 2021-04-06 | 福建省隆丰生物科技有限公司 | External composition for losing weight and reducing fat and preparation method thereof |
Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4613672A (en) * | 1983-07-05 | 1986-09-23 | Mitsu Norin Co., Ltd. | Process for the production of tea catechins |
US4673530A (en) * | 1983-05-30 | 1987-06-16 | Mitsui Norin Co., Ltd. | Process for the production of a natural antioxidant obtained from tea leaves |
US5605929A (en) * | 1992-05-27 | 1997-02-25 | Arch Development Corp. | Methods and compositions for inhibiting 5α-reductase activity |
US5827886A (en) * | 1997-05-07 | 1998-10-27 | Thione International, Inc. | Composition for relief of arthritis-induced symptoms |
US5879683A (en) * | 1994-03-04 | 1999-03-09 | Royal Free Hospital School Of Medicine | Antibacterial agent containing tea extract or active fraction thereof and β-lactam antibiotic |
US6210679B1 (en) * | 1999-01-07 | 2001-04-03 | Hauser, Inc. | Method for isolation of caffeine-free catechins from green tea |
US6214868B1 (en) * | 2000-02-29 | 2001-04-10 | Sam-A Pharm. Co., Ltd. | Method for preventing or treating coronary restenosis with catechin |
US6242010B1 (en) * | 1999-07-21 | 2001-06-05 | Thione International, Inc. | Synergistic antioxidant compositions in management of hemorrhoids and other ano-rectal inflammatory conditions |
US6277396B1 (en) * | 2000-05-11 | 2001-08-21 | Maximum Human Performance, Inc. | Dietary supplement containing a thermogenic substance and an adrenal support substance |
US6410052B1 (en) * | 1999-03-30 | 2002-06-25 | Purdue Research Foundation | Tea catechins in sustained release formulations as cancer specific proliferation inhibitors |
US6410061B1 (en) * | 1999-03-30 | 2002-06-25 | Purdue Research Foundation | Tea catechins as cancer specific proliferation inhibitors |
US6428818B1 (en) * | 1999-03-30 | 2002-08-06 | Purdue Research Foundation | Tea catechin formulations and processes for making same |
US6451328B1 (en) * | 2000-08-03 | 2002-09-17 | Color Access, Inc. | Antioxidants in clusters of structured water |
US6531162B1 (en) * | 2002-07-30 | 2003-03-11 | William Charles Llewellyn | Adrenergically-mediated weight loss product |
US6576660B1 (en) * | 1997-10-31 | 2003-06-10 | Arch Development Corporation | Methods and compositions for regulation of 5-α-reductase activity |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE60031921T2 (en) * | 1999-08-16 | 2007-09-20 | Dsm Ip Assets B.V. | Process for the preparation of epigallocatechin gallate |
-
2003
- 2003-07-08 US US10/615,887 patent/US20050008712A1/en not_active Abandoned
- 2003-07-30 WO PCT/US2003/024155 patent/WO2005014020A1/en active Application Filing
- 2003-07-30 AU AU2003258003A patent/AU2003258003A1/en not_active Abandoned
Patent Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4673530A (en) * | 1983-05-30 | 1987-06-16 | Mitsui Norin Co., Ltd. | Process for the production of a natural antioxidant obtained from tea leaves |
US4613672A (en) * | 1983-07-05 | 1986-09-23 | Mitsu Norin Co., Ltd. | Process for the production of tea catechins |
US5605929A (en) * | 1992-05-27 | 1997-02-25 | Arch Development Corp. | Methods and compositions for inhibiting 5α-reductase activity |
US5879683A (en) * | 1994-03-04 | 1999-03-09 | Royal Free Hospital School Of Medicine | Antibacterial agent containing tea extract or active fraction thereof and β-lactam antibiotic |
US5827886A (en) * | 1997-05-07 | 1998-10-27 | Thione International, Inc. | Composition for relief of arthritis-induced symptoms |
US6576660B1 (en) * | 1997-10-31 | 2003-06-10 | Arch Development Corporation | Methods and compositions for regulation of 5-α-reductase activity |
US6210679B1 (en) * | 1999-01-07 | 2001-04-03 | Hauser, Inc. | Method for isolation of caffeine-free catechins from green tea |
US6410052B1 (en) * | 1999-03-30 | 2002-06-25 | Purdue Research Foundation | Tea catechins in sustained release formulations as cancer specific proliferation inhibitors |
US6410061B1 (en) * | 1999-03-30 | 2002-06-25 | Purdue Research Foundation | Tea catechins as cancer specific proliferation inhibitors |
US6428818B1 (en) * | 1999-03-30 | 2002-08-06 | Purdue Research Foundation | Tea catechin formulations and processes for making same |
US6242010B1 (en) * | 1999-07-21 | 2001-06-05 | Thione International, Inc. | Synergistic antioxidant compositions in management of hemorrhoids and other ano-rectal inflammatory conditions |
US6214868B1 (en) * | 2000-02-29 | 2001-04-10 | Sam-A Pharm. Co., Ltd. | Method for preventing or treating coronary restenosis with catechin |
US6277396B1 (en) * | 2000-05-11 | 2001-08-21 | Maximum Human Performance, Inc. | Dietary supplement containing a thermogenic substance and an adrenal support substance |
US6451328B1 (en) * | 2000-08-03 | 2002-09-17 | Color Access, Inc. | Antioxidants in clusters of structured water |
US6531162B1 (en) * | 2002-07-30 | 2003-03-11 | William Charles Llewellyn | Adrenergically-mediated weight loss product |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070292560A1 (en) * | 2004-06-24 | 2007-12-20 | Danyi Quan | Green tea formulations and methods of preparation |
US7815960B2 (en) * | 2004-06-24 | 2010-10-19 | Danyi Quan | Green tea formulations |
US20060173070A1 (en) * | 2005-01-31 | 2006-08-03 | Kao Corporation | Method of enhancing motor function |
US20070116788A1 (en) * | 2005-01-31 | 2007-05-24 | Kao Corporation | Method of enhancing motor function |
EP1885453A1 (en) * | 2005-06-03 | 2008-02-13 | Horizon Science Pty. Ltd. | Substances having body mass redistribution properties |
EP1885453A4 (en) * | 2005-06-03 | 2011-06-29 | Horizon Science Pty Ltd | Substances having body mass redistribution properties |
US20070178216A1 (en) * | 2006-02-02 | 2007-08-02 | Chithan Kandaswami | Composition and method for promoting weight loss |
US20070178176A1 (en) * | 2006-02-02 | 2007-08-02 | Chithan Kandaswami | Composition and method for promoting weight loss |
US7989009B2 (en) | 2006-02-02 | 2011-08-02 | Advocare International, L.P. | Composition and method for promoting weight loss |
EP3285789A4 (en) * | 2015-04-24 | 2019-01-23 | Grethe Stoa Birketvedt | Plant extracts for the treatment of excess weight and obesity |
Also Published As
Publication number | Publication date |
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AU2003258003A1 (en) | 2005-02-25 |
WO2005014020A1 (en) | 2005-02-17 |
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